|
2
|
16
|
2gphB |
Docking motif interactions in the map kinase erk2 |
|
51
|
147
|
2g6zA |
Crystal structure of human dusp5 |
|
0
|
11
|
2fysC |
Crystal structure of erk2 complex with kim peptide derived from mkp3 |
|
193
|
576
|
2fh7A |
Crystal structure of the phosphatase domains of human ptp sigma |
|
98
|
290
|
2g59A |
Crystal structure of the catalytic domain of protein tyrosine phosphatase from homo sapiens |
|
56
|
147
|
2fekA |
Structure of a protein tyrosine phosphatase |
|
97
|
289
|
2fjnA |
The structure of phosphotyrosine phosphatase 1b in complex with compound 2 |
|
98
|
289
|
2fjmA |
The structure of phosphotyrosine phosphatase 1b in complex with compound 2 |
|
109
|
297
|
2f6vA |
Protein tyrosine phosphatase 1b with sulfamic acid inhibitors |
|
112
|
297
|
2f6tA |
Protein tyrosine phosphatase 1b with sulfamic acid inhibitors |
|
108
|
297
|
2f70A |
Protein tyrosine phosphatase 1b with sulfamic acid inhibitors |
|
112
|
297
|
2f71A |
Protein tyrosine phosphatase 1b with sulfamic acid inhibitors |
|
107
|
297
|
2f6wA |
Protein tyrosine phosphatase 1b with sulfamic acid inhibitors |
|
110
|
297
|
2f6yA |
Protein tyrosine phosphatase 1b with sulfamic acid inhibitors |
|
110
|
297
|
2f6zA |
Protein tyrosine phosphatase 1b with sulfamic acid inhibitors |
|
107
|
302
|
2f6fA |
The structure of the s295f mutant of human ptp1b |
|
60
|
162
|
2esbA |
Crystal structure of human dusp18 |
|
9
|
134
|
2edxA |
Solution structures of the fn3 domain of human receptor-type tyrosine-protein phosphatase f |
|
7
|
94
|
2e5kA |
Solution structure of sh3 domain in suppressor of t-cell receptor signaling 1 |
|
7
|
103
|
2edyA |
Solution structures of the fn3 domain of human receptor-type tyrosine-protein phosphatase f |
|
44
|
150
|
2e0tA |
Crystal structure of catalytic domain of dual specificity phosphatase 26, ms0830 from homo sapiens |
|
7
|
121
|
2dlhA |
Solution structure of the second fn3 domain of human receptor-type tyrosine-protein phosphatase delta |
|
61
|
158
|
2dxpA |
Crystal structure of the complex of the archaeal sulfolobus ptp-fold phosphatase with phosphopeptides a-(p)y-r |
|
7
|
104
|
2dleA |
Solution structure of the fourth fn3 domain of human receptor-type tyrosine-protein phosphatase eta |
|
11
|
107
|
2dn7A |
Solution structures of the 6th fn3 domain of human receptor-type tyrosine-protein phosphatase f |
|
11
|
106
|
2djuA |
Solution structures of the fn3 domain of human receptor-type tyrosine-protein phosphatase f |
|
107
|
297
|
2cm8A |
Structural basis for inhibition of protein tyrosine phosphatase 1b by isothiazolidinone heterocyclic phosphonate mimetics |
|
87
|
302
|
2cfvA |
Crystal structure of human protein tyrosine phosphatase receptor type j |
|
104
|
296
|
2cngA |
Structural insights into the design of nonpeptidic isothiazolidinone- containing inhibitors of protein tyrosine phosphatase 1b |
|
88
|
274
|
2cm3A |
Structure of protein tyrosine phosphatase 1b (c2) |
|
103
|
286
|
2cneA |
Structural insights into the design of nonpeptidic isothiazolidinone- containing inhibitors of protein tyrosine phosphatase 1b |
|
10
|
64
|
2cpwA |
Solution structure of rsgi ruh-031, a uba domain from human cdna |
|
102
|
296
|
2cmaA |
Structural basis for inhibition of protein tyrosine phosphatase 1b by isothiazolidinone heterocyclic phosphonate mimetics |
|
103
|
283
|
2cm2A |
Structure of protein tyrosine phosphatase 1b (p212121) |
|
101
|
296
|
2cnfA |
Structural insights into the design of nonpeptidic isothiazolidinone- containing inhibitors of protein tyrosine phosphatase 1b |
|
105
|
296
|
2cnhA |
Structural insights into the design of nonpeptidic isothiazolidinone- containing inhibitors of protein tyrosine phosphatase 1b |
|
102
|
285
|
2cmcA |
Structural basis for inhibition of protein tyrosine phosphatase 1b by isothiazolidinone heterocyclic phosphonate mimetics |
|
9
|
119
|
2cs5A |
Solution structure of pdz domain of protein tyrosine phosphatase, non-receptor type 4 |
|
104
|
296
|
2cm7A |
Structural basis for inhibition of protein tyrosine phosphatase 1b by isothiazolidinone heterocyclic phosphonate mimetics |
|
104
|
299
|
2cniA |
Structural insights into the design of nonpeptidic isothiazolidinone- containing inhibitors of protein tyrosine phosphatase 1b |
|
100
|
286
|
2cmbA |
Structural basis for inhibition of protein tyrosine phosphatase 1b by isothiazolidinone heterocyclic phosphonate mimetics |
|
96
|
286
|
2cjzA |
Crystal structure of the c472s mutant of human protein tyrosine phosphatase ptpn5 (step, striatum enriched phosphatase) in complex with phosphotyrosine |
|
95
|
291
|
2c7sA |
Crystal structure of human protein tyrosine phosphatase kappa at 1.95a resolution |
|
94
|
290
|
2bzlA |
Crystal structure of the human protein tyrosine phosphatase n14 at 1. 65 a resolution |
|
44
|
259
|
2c9aA |
Crystal structure of the mam-ig module of receptor protein tyrosine phosphatase mu |
|
102
|
282
|
2bv5A |
Crystal structure of the human protein tyrosine phosphatase ptpn5 at 1.8a resolution |
|
138
|
525
|
2b3oA |
Crystal structure of human tyrosine phosphatase shp-1 |
|
95
|
291
|
2b4sA |
Crystal structure of a complex between ptp1b and the insulin receptor tyrosine kinase |
|
105
|
297
|
2bgdA |
Structure-based design of protein tyrosine phosphatase-1b inhibitors |
|
105
|
297
|
2azrA |
Crystal structure of ptp1b with bicyclic thiophene inhibitor |
